Hybridoma antibody which binds IL-2 receptor

ABSTRACT

A monoclonal antibody which specifically binds to the human IL-2 receptor, and a hybridoma which produces the antibody, are disclosed.

CROSS-REFERENCE TO RELATED APPLICATIONS

This is a continuation of U.S. patent application Ser. No. 825,360, filed Feb. 2, 1986, now abandoned, which is a continuation of U.S. patent appllication Ser. No. 612,559, filed May 21, 1984, now U.S. Pat. No. 4,578,335.

TECHNICAL FIELD

The present invention relates to interleukin 2 receptor, and more particularly to a hybridoma which secretes a monoclonal antibody capable of binding to interleukin 2 receptor.

BACKGROUND OF THE INVENTION

Many normal immune responses require participation by T-cells. T-cell proliferation is controlled by the presence of a polypeptide growth hormone, interleukin 2 (hereinafter IL-2), formerly known as T-cell growth factor (TCGF). See Gillis and Smith, Nature 28: 154 (1977). The mechanism by which IL-2 controls T-cell growth is not completely understood. However, it is known that IL-2 acts on T-cells via a specific, high affinity plasma membrane receptor. In order to continue to divide, IL-2 dependent T-cells must express this receptor and IL-2 must bind to a portion of this receptor. Robb, et al., J. Exp. Med. 154: 1455 (1981). A more complete knowledge of the biochemistry of the IL-2 receptor would foster a better understanding of the interaction between IL-2 and T-cells. To date this has been hampered, at least in part, by the unavailability of IL-2 receptor in purified form.

Leonard, et al, Nature 300: 267 (1982), reported employing a murine monoclonal antibody, designated anti-Tac, to significantly block the binding of radiolabeled IL-2 to the human lymphoma T-cell line, HUT-102. This antibody resulted from immunization of mice with long term cultures of human T-cells. The anti-Tac antibody was reported to bind to a glycoprotein receptor having a molecular weight of about 47,000-53,000 daltons, and also to proteins having molecular weights of about 113,000 and 180,000 daltons. Leonard, et al., suggested that the cell surface determinant (i.e., the 47,000-53,000 molecular weight protein) to which the anti-Tac antibody bound to was the IL-2 receptor.

Robb and Green, J. Exp. Med. 158: 1332 (1983), reported use of anti-Tac antibody in conjunction with mitogen-activated normal lymphocytes to immunoprecipitate a protein having a molecular weight of about 52,000-57,000 daltons. They found that this same protein also bound to IL-2.

Leonard, et al., Proc. Natl. Acad. Sci. USA 80: 6957 (1983), observed that receptors recognized by anti-Tac antibody on HUT-102 cells and on phytohemagglutinin-activated normal T-cells appeared to be larger on reducing gels than on nonreducing gels, thus suggesting the presence of intrachain disulfide bonds. Also, the HUT-102 cell receptor was reported to exhibit an isoelectric point of from 5.5 to 6.0. From post-translational studies, Leonard, et al., suggested that the HUT-102 receptor is composed of a peptide backbone of 33,000 molecular weight that is initially glycosylated by an N-linked mechanism to achieve a 35,000-37,000 molecular weight doublet and then glycosylated by an O-linked mechanism to increase the weight of the molecule by about 13,000-15,000 daltons.

SUMMARY OF THE INVENTION

The present invention provides a specific monoclonal antibody secreted by hybridoma 2A3 (ATCC HB 8555) that binds an epitope on the IL-2 receptor molecule with high affinity.

DETAILED DESCRIPTION

Preparation of IL-2 Receptor Extracts From Malignant and Normal Cells

Malignant cells are cultured in vitro in a suitable culture medium supplemented with serum and various additives. After an optimum culture period, the cells are harvested and IL-2 receptor containing extracts formed from the cells. The malignant cell lines which may be employed as a source of IL-2 receptors include T-lymphoma or T-leukemia cell lines. These cell lines are produced by either a spontaneous occurrence, via viral transformation or via transformation by chemical carcinogen or irradiation. The present invention has been carried out in conjunction with a naturally occurring lymphoma cell line, designated HUT-102. The cell line is available from a wide variety of sources and has been used extensively by researchers.

The numbers of IL-2 receptors expressed by stimulation of peripheral blood leukocytes with a plant mitogen varies with time. Optimum levels of IL-2 receptor expression are reached approximately 72 hours after mitogen stimulation.

The culture medium used to expand the IL-2 receptor bearing malignant cells may consist of commercially available medium, such as Roswell Park Memorial Institute medium (RPMI), Dulbecco's Modified Eagle Medium (DMEM) and Click's Medium. Additives, which may be individually or in combination added to the culture medium, include serum, such as fetal calf serum (FCS) or normal human serum. Additional additives include glutamine and various antibiotics, such as penicillin and streptomycin.

The process of culturing the malignant and normal cells to induce receptor formation may be carried out in various environmental conditions. Preferably, however, cultures are maintained in the temperature range of approximately 35°-38° C. in a humidified atmosphere of approximately 5-10% CO₂ in air. Also, culture pH should be kept in slightly alkaline condition, in the range of approximately pH 7.0-7.4.

IL-2 receptor containing extracts are prepared from cultivated normal and malignant cells by harvesting the cells by centrifugation. The cells are then washed with a buffered saline solution and resuspended in the buffered saline solution together with a detergent and phenylmethylsulfonylfluoride (PMSF). After a period of time the detergent extract is centrifuged to remove nuclei and insoluble debris and then is stored frozen until used.

Preparation of Monoclonal Antibody Against IL-2 Receptor

The present invention provides a monoclonal antibody having a high affinity to an epitope on the IL-2 receptor molecule. The antibody is used as a bound ligand in the affinity chromatography procedures during purification of the IL-2 receptor. The antibody is also employed in a radioimmune precipitation assay and in soluble receptor assays to monitor the IL-2 receptor protein during purification steps, as more fully discussed below.

A preferred procedure for generating the monoclonal antibody against the IL-2 receptor is generally disclosed in U.S. Pat. No. 4,411,993, incorporated herein by reference. In the procedure, BALB/c mice are injected with PHA activated human peripheral blood leukocytes (PHA/PBL) several times at weekly intervals. Prior to the first injection, the PHA/PBL is emulsified in complete Freund's adjuvant and prior to the remainder of the injections the PHA/PBL is emulsified in incomplete Freund's adjuvant.

During the course of immunization, serum samples from the mice are tested by an enzyme linked immunoabsorbant assay (ELISA), as is well known in the art, for the presence of antibody reaction with the immunization cells. Once an antibody titer is detected, the animals are given an intravenous injectoion of PHA/PBL suspended in saline. Several days later the animals are sacrificed and their spleens harvested. Single cell suspensions from the splenocytes are cultured in tissue medium supplemented with various additives to expand the number of antibody producing cells. The antibody producing cells are isolated from the culture and purified by standard techniques for subsequent fusion with myeloma cells to produce hybrid cells that express anti-IL-2 receptor antibody. The fusion process is detailed in U.S. Pat. No. 4,411,933 and in Nowinski, et al., Virology 93: 111 (1979), incorporated herein by reference.

After fusion, the hybrid cells are resuspended in a tissue culture medium supplemented with various additives and selected suppressing agents to preclude the growth of unfused myeloma cells, double myeloma cells, unfused spleen cells and double spleen cell hybrids, thereby liberating the anti-IL-2 receptor antibody producing cells. Such growth inhibitors or suppressants may include hypoxanthine, aminopterin and thymidine (hereinafter collectively referred to as HAT).

After several days of culture, the hybridoma cells which are generated are screened by ELISA assay for anti-IL-2 receptor antibody responses. These hybrid cells are tested for production of antibody capable of inhibiting both mitogen and antigen induced proliferation of human peripheral blood leukocytes. The hybrid cells which give positive ELISA results are gradually weaned to HAT-free medium and then cultured in vitro in large volumes for bulk production of antibody. Alternatively, the cells may be expanded in vivo by injecting the hybridoma cells in the peritoneal cavities of mice and thereafter collecting the intraperitoneal ascites which contain high concentrations of the antibody. The antibodies contained in the ascites fluid can be isolated and concentrated by established techniques, such as by ammonium sulfate precipitation followed by gel column chromatography. If required, the antibody can be further purified by ion exchange chromatography and/or affinity chromatography. By the above process, a particular hybridoma, designated as 2A3, was found to produce antibody that significantly inhibited both mitogen and antigen induced proliferation of human peripheral blood leukocytes.

The present invention concerns potent cell line sources of anti-IL-2 receptor antibody by cloning cell lines known to produce this antibody, for instance, the 2A3 cell line. The cloning is accomplished by the limiting dilution procedure, as is well known in the art and as is detailed in U.S. Pat. No. 4,411,993. By this procedure, one particular subclone, designated 2A3-A1H, was found to produce antibody that almost entirely inhibited both mitogen and antigen induced proliferation of human peripheral blood leukocytes. The 2A3-A1H antibody has been characterized as of the γ₁ K isotype with an unusually high affinity to the human IL-2 receptor. The 2A3 hybridoma cell line has been deposited with the American Type Culture Collection, Rockville, Md., USA, (ATCC) under accession number ATCC HB 8555.

A control antibody preferably is employed to confirm the processes of the present invention utilizing anti-IL-2 receptor antibody and as a reagent in the purification of the receptor. The control antibody should be of the same isotype as the anti-IL-2 receptor antibody. Applicants have identified the antibody secreted by the mouse myeloma cell line MOPC-21 as a suitable control antibody for the 2A3-A1H antibody. The MOPC-21 cell line is widely available from numerous private and commercial sources.

Soluble IL-2 Receptor Assays

Assays employing the 2A3-A1H monoclonal antibody are used in conjunction with the present invention to monitor the quantitative amount of IL-2 receptor present in the initial cell lysates and during purification procedures. These assays hinge on the discovery by applicants that the 2A3-A1H antibody has an extremely high affinity for the IL-2 receptor, the affinity constant being in excess of 5×10⁹ per M⁻¹ and that the 2A3-A1H antibody can be radioiodinated to high specific activity and still retain its capacity to bind to the IL-2 receptor.

One such preferred assay involves ascertaining the extent to which samples of cell lysate or column chromatography fractions containing IL-2 receptors are capable of inhibiting the binding of radiolabeled IL-2 antibody to glutaraldehyde fixed, intact receptor bearing cells. This assay relies on the observation by applicants that IL-2 receptor is stable to glutaraldehyde fixation, i.e., the receptor cannot be extracted from such cells with nonionic detergents, such as Triton X-100, and the presence of detergent does not affect the binding of radiolabeled 2A3-A1H antibody to the fixed cells. Preincubation of a subsaturating dose of iodinated 2A3-A1H antibody with detergent solutions containing the IL-2 receptor inhibits the subsequent binding of the 2A3-A1H antibody to the glutaraldehyde fixed cells. This assay will hereinafter be referred to as the soluble inhibition assay.

For use in the soluble inhibition assay, the 2A3-A1H antibody is radiolabeled with iodine 125 (¹²⁵ I) by a chloramine-T method, as is well known in the art and as described by Segal and Hurwitz, J. Immunol. 118: 1338 (1977). The standard labeling conditions employed are: 50 μg 2A3-A1H IgG; 4 nmoles of chloramine-T (Sigma Chemical Company, St. Louis, MO); and, 2.5 mCi of ¹²⁵ I sodium iodide (New England Nuclear, Boston, MA), in a final volume of 60 μl. This protocol has resulted in preparations of ¹²⁵ I-2A3-A1H, which routinely have specific activities in the range of 2 to 5×10¹⁵ cpm/mmole (1.3-3.3×10⁷ cpm/μg). Also, 2A3-A1H antibodies labeled in this way were found to be more than 95 percent bindable to IL-2 receptor bearing cells and had apparent affinity constants in excess of 5×10⁹ M⁻ 1.

In the soluble inhibition assay, 50 μl of ¹²⁵ I-2A3-A1H (2×10⁻¹⁰ M) is mixed with 50 μl of an appropriate dilution of cell lysate or column fraction in phosphate buffered saline (PBS) containing 1% (w/v) Triton X-100 detergent (Sigma Chemical Company, St. Louis, MO) in RPMI-1640 medium containing 2% bovine serum albumin (BSA), 20 mM HEPES buffer (pH 2.7) and 0.2% sodium azide (binding medium). This mixture is incubated for one hour at room temperature in round bottom 96 well plates (Linbro, Hamden, CT). At the end of the incubation period, 10⁷ glutaraldehyde fixed, PHA activated human T-cells in 50 μl of binding medium are added to detect uncomplexed ¹²⁵ I-2A3-A1H. Incubation is continued for one hour at room temperature. Duplicate 60 μl aliquots of the mixture are then transferred to precooled 400 μl polyethylene centrifuge tubes containing 200 μl of a phthalate oil mixture and the cell bound antibody is separated from unbound antibody by centrifugation. The details of the well-known phthalate oil separation method are set forth in Segal and Hurwitz, supra. The percent of specific inhibition caused by the lysate or column fraction is calculated by using 50 μl of PBS-2% Triton X-100 instead of a test sample for the positive control. Also, 15 μl of PBS-2% Triton X-100 containing 10⁻⁸ M unlabeled 2A3-A1H is used as a negative control.

The nitrocellulose dot assay (dot assay) is used as a second soluble IL-2 receptor assay to quantify the amount of IL-2 receptor molecules present in a sample of cell lysate or column fraction. Briefly, in the dot assay, solutions are made of a log₂ dilution series of potential IL-2 receptor containing samples and PBS containing 1% Triton-100. Samples of 5 μl of these solutions are then applied to a piece of dry nitrocellulose (Schleicher and Schvell, Keene, N.H.). The nitrocellulose is incubated for one hour at room temperature in 10 ml of TBS-3% BSA containing 0.05 μg/ml ¹²⁵ I-2A3-A1H and 0.6 μg/ml unlabeled MOPC-21. The nitrocellulose is then washed three times in TRIS buffered saline and twice in TRIS buffered saline containing 1% (w/v) Nonidet P-40 detergent (Gollaro Schlesinger Chemical Manufacturing Corp., Carl Place, N.Y.), 1% (w/v) sodium deoxycholate, and 0.1% (w/v) sodium lauryl sulfate. Each of these washes lasts 30 minutes at room temperature. After the final wash, the nitrocellulose sheet is blotted dry, covered with a clear plastic sheet and then exposed at -70° C. to Kodak X-omat AR film.

Radioimmune Precipitation Assay

The specificity of the IL-2 receptor antibody is ascertained with a radioimmune precipitation assay involving forming precipitations between samples of radiolabeled IL-2 receptor molecules and an antibody to the receptor and then employing polyacrylamide gel electrophoresis and either fluorography or autoradiography to visualize the receptor proteins that were precipitated. In this assay technique, the IL-2 receptor molecules are labeled either by surface iodination after extraction or metabolically before extraction.

Radiolabeling of the IL-2 receptor cell membranes after extraction is performed by the ¹²⁵ I-IODO-GEN method (Pierce Chemical, Rockford, IL). The details of this radiolabeling technique are well known in the art and described by Urdal, et al., Cancer Metastasis Reviews 1: 65 (1982); and, Markwell, et al., Biochemistry 17: 4807 (1978). The use of ³⁵ S methionine to label the receptor molecules metabolically also is well known in the art and is described by, for instance, Robb and Greene, J. Exp. Med. 58: 1332 (1983).

After labeling with ¹²⁵ I or ³⁵ S methionine, the cells are washed with PBS and then extracted with PBS containing 1% Triton X-100 and 2 mM PMSF. Affinity supports for the radioimmune precipitation assay are prepared by coupling purified antibodies (2A3-A1H and MOPC-21) to Affi-gel-10. Briefly, one volume of moist Affi-gel-10 is added to one volume of antibody (3-5 mg/ml) in borate buffered saline (BBS) and then the mixture incubated overnight at 4° C. Thereafter, 100 μl of 1M glycine ethylester is added per ml of gel to couple any of the unreacted groups on the Affi-gel-10. Applicants have found that routinely from 3 to 4 mg of antibody are coupled per ml of the gel. Before use, each gel is washed extensively with PBS. Each gel is also washed with a buffer solution composed of PBS-1% Triton X-100 and 0.5M TRIS, pH 7.5, containing 0.5M NaCl, 1% (w/v) NP 40 detergent, 1% (w/v) sodium deoxycholate, and 0.1% sodium dodecyl sulfate (SDS) (RIPA buffer).

The radioimmune precipitations are performed by mixing 50 μl of radiolabeled cell extract with 75 μl of PBS-1% Triton X-100 containing 20% (v/v) of affinity gel having antibody coupled thereto. The mixture is incubated overnight at 4° C. and then the gel washed four times with RIPA buffer and twice with 0.1M TRIS, pH 8.0, containing 0.5M NaCl, 5 mM ethylenediamine tetraacetate (EDTA), and 0.5% NP-40 detergent. After the final wash, the resultint gel pellets are suspended in 40 μl of SDS polyacrylamide gel sample buffer (0.06M TRIS, pH 6.8, 2% SDS, 10% glycerol, 5% 2-mercaptoethanol and boiled for three minutes to break apart the bonds between the antibody and the IL-2 receptor molecules. A 30 μl sample of the supernate is then analyzed by SDS-Polyacrylamide gel electrophoresis (PAGE) (8% polyacrylamide gel for ¹²⁵ I labeled receptor; 12% polyacrylamide gel for ³⁵ S methionine labeled receptor) according to the stacking gel procedure of Laemmli, Nature 227: 680 (1970). Receptor proteins are visualized on gels by autoradiography.

Gel Electrophoresis of Chromatography Column Fractions

Fractions eluted from the affinity chromatography and reversed phase HPLC columns employed in the purification processes of the present invention are assayed by gel electrophoresis. 50 μl aliquots were removed from the eluate fractions. The aliquots are dried under vacuum after addition of 2 μl of 10% SDS (w/v) to each aliquot. The dried residue is dissolved in 40 μl of SDS polyacrylamide gel sample buffer and then boiled for 3 minutes. The solution is applied to an 8% polyacrylamide gel and electrophoresis is then carried out by the stacking gel procedure of Laemmli, supra. The resulting gel samples are silver stained by the method described by Oakley, et al., Anal. Biochem. 105: 361 (1980).

Purification of IL-2 Receptor

Cell extracts from the malignant and normal cells produced by the above procedures are initially concentrated by affinity chromatography techniques employing the same affinity supports used in the radioimmune precipitation assay described above. The procedure employed involves applying cell extracts first to an MOPC-21 column and then to a second column prepared from a mixture of MOPC-21 antibody and 2A3-A1H antibody so that in the second column from 3 to 4 mg of total IgG is coupled to each ml of gel, but only 10 to 30% of the antibody is composed of 2A3-A1H. This technique is used to counteract the extremely high affinity between the 2A3-A1H antibody and the IL-2 receptor.

In the purification procedure, the cell extracts, as prepared above, are first applied to the MOPC-21 column that has been preequilibrated with an appropriate buffer containing a detergent, thereby to remove proteins in the cell extract that might nonspecifically bind to mouse immunoglobulin. The flow through from the MOPC-21 column is then applied to the 2A3-A1H column. Elution is carried out with an appropriate saline-detergent solution. The recovered fractions are then dialyzed against decreasing concentrations of the eluting agent to optimize the recovery of biological activity.

Fractions are collected and assayed by gel electrophoresis and silver staining, as described above. Applicants have found that by use of the affinity chromatography procedure, IL-2 receptor from malignant cells which constitutively produce the receptor is purified approximately 1600 times from initial cell lysate. A somewhat lower purification level is typically attained for IL-2 receptor from activated normal cells.

The pooled active fractions from the above affinity chromatography procedure is employed as a starting material for the HPLC procedures. The HPLC technique used in the present invention preferably employs a reversed phase, tetra methyl bonded silica column having a pore size sufficiently large to be optimally utilized with the proteinaceous IL-2 receptor, i.e., a pore size of at least 300 A.

Suitable reversed phase HPLC columns for use in the practice of the present invention are articles of commerce. A preferred column for this purpose is the Vydac C-4 reversed phase column commercially available from Separations Group, Hesperia, CA. This column consists of tetra methyl silane groups covalently bonded by means of a siloxane (silicon-oxygen-silicon) bond to the surface of the 300 A pore diameter silica gel which has been classified to a mean particle size of 5 microns.

The elution of the proteins from the HPLC column is carried out in a manner well-known in the art. A suitable elution procedure for removing the bonded receptor molecule proteins from the tetra methyl column involves the use of a linear gradient of the acetonitrile. A preferred gradient for this purpose is 0 to 95% (v/v) acetonitrile gradient in trifluoroacetic acid (TFA), pH 2.1.

The eluted protein can be conveniently monitored with detection systems that are well-known in the art. For example, an automated fluorescence detection system as described by Stein and Moschera, Methods Enzymol. 78: 435 (1981), may be employed. Alternatively, the relative protein concentration in the fractions eluted from the HPLC columns can be determined by measuring absorbance of the eluted material in an automated ultraviolet light spectrophotometer, at 214 nanometers light wave length. The suitable automated ultraviolet light absorbance detection apparatus is available from Waters Associates, Milford, MA.

By use of the above described soluble receptor assay techniques, applicants have found that the specific activity of the IL-2 receptor after HPLC purification is very high, i.e., approximately 21,000 femtomole (fm) IL-2 receptor/μg protein for IL-2 receptor derived from malignant cells. This is approximately a 16,700 fold level of purification over the specific activity of the IL-2 receptor in the starting cell lysate. The specific activity of the IL-2 receptor from normal T-cells was about 1/3 of the specific activity from malignant cells. By polyacrylamide gel electrophoresis and silver staining, applicants ascertained that the molecular weight of the IL-2 receptor from normal cells is approximately 60,000 daltons, as opposed to 55,000 daltons for receptor molecules found constitutively on the malignant cells.

Amino Acid Sequencing

The ability to prepare homogeneous IL-2 receptor has permitted applicants to determine the amino acid composition and sequence of the amino terminal portion of this molecule. This information may be employed to assist in the cloning of the IL-2 receptor gene and the production of large quantities of pure IL-2 receptor for clinical trials and ultimately for widespread medical use. Moreover, the availability of homogeneous IL-2 receptor will no doubt lead to a more complete understanding of the biology of IL-2.

Samples of homogeneous IL-2 receptor, as prepared above, can be analyzed for amino acid composition and sequence, for instance with an automated sequencer, such as with an Applied Biosystems model 470A protein sequencer. Ideally, several sequencing runs are made to confirm the accuracy of the sequence. Through this technique, applicants have found that the first 15 residues of the amino terminal portion of the IL-2 receptor molecules are composed of the following sequence: Glu-Leu-Cys-Asp-Asp-Asp-Pro-Pro-Glu-Ile-Pro-His-Ala-Thr-Phe.

The processes and products of the present invention are further illustrated by the following examples.

EXAMPLE 1

Preparation of IL-2 Receptor-Containing Extracts From Malignant Cell Line

HUT-102 cells in a concentration of 2×10⁵ cells per ml are cultured in 100-500 ml volumes in various plastic culture flasks or bottles (Falcon Plastics, Oxnard, CA) in RPMI-1640 medium. The medium is supplemented with 10% FCS, 2 mM glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin. Since the HUT-102 cells have been reported to produce human T-cell leukemia virus (HTLV-1), work with this cell line is performed in a P-3 isolation facility.

The cells are cultured for 3-5 days in a humidified atmosphere of 5% CO₂ in air. After this period of time, viable cells are harvested by centrifugation and washed three times in PBS. Thereafter, the cell pellet is suspended in a volume that is three times the volume of the cell pellet in a solution composed of PBS containing 1% (w/v) Triton X-100 detergent and 2 Mm PMSF. This mixture is kept on ice and periodically vortexed for 30 minutes. The extract was then centrifuged at 20,000×g for 20 minutes to remove nuclei and insoluble debris. The cell extract, as thus prepared, is then stored at -70° C. until used.

EXAMPLE 2

Preparation of IL-2 Receptor-Containing extracts From Lectin Activated Normal Cells

Human peripheral blood mononuclear cells are prepared by Ficoll-Hypaque density gradient centrifugation as described by Boyum, supra. Briefly, enriched T-cells are obtained by rosetting with neuraminidase-treated sheep erythrocytes. The resulting rosetting (E⁺ () and nonrosetting (E⁻) cells are incubated separately in 100-mm plastic petri dishes in 8% FCS at a concentration of 2-5×10⁶ per ml. The adherent E⁻ cells are recovered with a rubber policeman after removing nonadherent cells with three media washes. The E⁻ adherent cells together with the E⁺ nonadherent cells in a ratio of 1:25 are placed in bulk culture in 75-cm² flasks at a concentration of about 1-2×10⁶ cells/ml in RPMI-1640 medium supplemented with 10% FCS, 100 U/ml penicillin and 100 μg/ml streptomycin. Activation is accomplished with 1% (v/v) PHA (Difco Laboratories, Detroit, MI). The cultures are incubated at 37° C. in a humidified atmosphere of 5% CO₂ in air. Aliquots containing approximately 1-2×10⁷ cells are removed at various times for analysis of cell surface IL-2 receptors.

Cells are harvested by centrifugation approximately 72 hours after mitogen stimulation, and washed three times with PBS. The resulting cell pellet is suspended in a volume three times the volume of the pellet in a solution composed of PBS containing 1% (w/v) Triton X-100 detergent and 2 mM PMSF. The resulting mixture is kept on ice with periodic vortexing for 30 minutes. Thereafter, the extract is centrifuged at 20,000×g for 20 minutes to remove nuclei and insoluble debris. The resulting cell extracts are stored at -70° C. until used.

EXAMPLE 3

Production of Monoclonal Antibody to IL-2 Receptor

Female BALB/c (Jackson Laboratories, Bar Harbor, ME) of ages from 8-12 weeks are immunized intradermally in the hind legs with 10⁷ PHA/PBL cells. Prior to immunization, the PHA/PBL cells are prepared as an emulsion by mixing these cells with 0.4 ml of complete Freund's adjuvant (Difco Laboratories, Detroit, MI). After the initial immunization, the mice are rechallenged weekly for four weeks with 10⁷ PHA/PBL cells in incomplete Freund's adjuvant.

Periodically, serum from the mice is collected and tested individually for binding to PHA/PBL by ELISA, in a manner well known in the art. The animals found to hve the highest response are given an additional intravenous injection of 10⁷ PHA/PBL in PBS. Four days later, the animals are sacrificed by cervical dislocation. The spleens of the animals are harvested and single cell suspensions prepared therefrom. The spleen cells are cultured in medium.

Fusion is achieved by mixing approximately 20×10⁶ spleen cells with approximately 10×10⁶ NS-1 murine myeloma cells in a 50 ml conical centrifuge tube. The cell mixture is pelleted by centrifugation for 5 minutes at 200×g, and then the supernate removed by aspiration. The centrifuge tube with its intact cell pellet is transferred into a 37° C. water bath. Then polyethylene glycol 15 w (Eastman, Inc.) 50% (w/v) in RPMI-1640 is added to the cell pellet in dropwise manner at a ratio of 1 ml of PEG/1.6×10⁸ spleen cells. Thereafter, one volume of RPMI-1640 and 10 volumes RPMI 1640 containing 15% FCS and 1 mM pyruvate are slowly added during gentle stirring. Then, the cell suspension is centrifuged at 200×g for 5 minutes and the supernate discarded to complete the fusion process.

The hybrid cells are selected by resuspending the resulting cell pellet in Click's medium containing 15% FCS and 100 mM sodium pyrate. The unfused myeloma driver cells (NS-2), double NS-1 hybrids, unfused spleen cells and double spleen cell hybrids are prevented from proliferation by the addition to the medium of approximately 13.6 mg/L of hypoxanthene, 0.176 mg/l aminopterin and 3.88 mg/L of thymidine. The suspension is then divided into 200 μl aliquots in flat-bottom microtiter plates (No. 3596, Costar Inc., Cambridge, MA). The cultures are maintained at approximately 37° C. in a humidified atmosphere of 5% CO₂ in air.

After 10 days of culture, a 100 μl aliquot of supernate is removed from each viable culture and tested in an ELISA assay for binding to PHA/PBL (IL-2 receptor positive) or PBL (IL-2 receptor negative). Hybrids which demonstrate significant binding to PHA/PBL and little or no binding to PBL are transferred to 1 ml cultures and gradually weaned to HAT-free media. These hybrids are subcloned by limiting dilution cultures. Through this process, applicants have identified one particular hybrid clone, designated as 2A3-A1H, which significantly inhibits both mitogen and antigen induced proliferation of human PBL. The 2A3-A1H monoclonal antibody has been characterized as of the γ₁ K isotype that exhibits a very high affinity to the human IL-2 receptor. This antibody inhibits the binding of IL-2 to its receptor and is antagonistic of IL-2 action.

EXAMPLE 4

In Vivo Production of Hybridoma Cells Producing Monoclonal Anti-IL-2 Receptor Antibodies

Anti-IL-2 receptor antibody was produced in high concentration in vivo by intraperitoneal injection of BALB/c mice with approximately 1-10×10⁶ hybridoma cells. One week prior to hybridoma cell injection, recipient BALB/c mice were given approximately 1.0 ml of pristane intraperitoneally as an ascites inducing irritant. From 8 to 14 days after hybridoma injection, intraperitoneal ascites were collected and each volume of fluid is mixed with 0.9 volume of 45% saturated ammonium sulfate and stirred overnight. The precipitate is separated by centrifugation and redissolved in phosphate buffer (0.05M), pH 6.8. Residual ammonium sulfate is removed by dialysis against the same buffer.

The protein solution is then passed over a 5 ml bed volume DE-52 column (Whatman, Clifton, NJ) and the fronting peak of protein is pooled. The pooled fractions are dialyzed against 0.02M sodium borate, 0.1M sodium NaCl, pH 8.5, (BBS) and then applied to a 2.6×90 cm ACA-34 (LKB, Bromma, Sweden) gel filtration column previously equilibrated in the same buffer. The fractions corresponding to IgG are collected and pooled. Yields typically are in the range of 3 mg IgG/ml of ascites.

EXAMPLE 5

Purification of IL-2 Receptor by Affinity Chromatography

Cell extracts from normal and malignant cells produced by the procedures of Examples 2 and 3 are concentrated by affinity chromatography technique employing an initial gel column having control antibody for removing protein that might nonspecifically bind to mouse IgG and a second column having 2A3-A1H antibody bound thereto. The control antibody used in the initial column is secreted by the myeloma cell line MOPC-21. This antibody is of the same isotype as the 2A3-A1H antibody and is readily available.

To prepare the columns, purified 2A-3-A1H and MOPC-21 antibodies are coupled to Affi-gel-10 (Biorad, Richmond, CA) according to the manufacturer's instructions. Equal volumes of moist Affi-gel-10 and antibody (3-5 mg/ml) in PBS are mixed together and incubated overnight at 4° C. Thereafter, unreacted sites on the Affi-gel-10 are blocked by addition of 100 μl of 1M glycine ethyl ester per ml of gel. Applicants found that the antibody-coupled gel routinely contained from 3 to 4 mg of antibody per ml of gel.

Because the 2A3-A1H antibody exhibits such an extremely high affinity for the IL-2 receptor, the receptor yield from the chromatography columns was improved by employing columns prepared with a mixture of MOPC-21 and 2A3-A1H antibody. A total of 3 to 4 mg IgG is coupled per ml of gel, of which only 10-30% of bound IgG is 2A3-A1H.

Prior to use, each gel is washed extensively with PBS and RIPA buffer. The MOPC-21 and 2A3-A1H gel columns are poured in 3 ml syringes that have their open ends closed with a cork and tubing, thereby to enable the columns to be run in either direction. The cell extracts, as prepared in Examples 1 and 2 above, are first applied to the MOPC-21 column at a flow rate of 0.1 ml/min at 4° C. to remove proteins that nonspecifically bind to the mouse IgG. This absorption is repeated once more and then the flow-through from the MOPC-21 column is twice applied to the 2A3-A1H column.

The 2A3-A1H column is then washed with 10 column volumes of PBS-1% Triton X-100, 10 column volumes of RIPA buffer and lastly, 10 column volumes of PBS-1% Triton X-100. Thereafter, the receptor is eluted from the column with 6M guanidine hydrochloride (GuHCl) and 0.5% Triton X-b 100. Eluate fractions in 1.2 ml volume are collected and each fraction is dialyzed against 3M GuHCl in 0.5% Triton X-100 for four hours. This is followed by dialysis against 1.5M GuHCl in 0.5% Triton X-100. Final dialysis is performed against PBS containing 0.5% Triton X-100. Aliquots at each stage of the purification are saved for analysis of biological activity by the above-described soluble receptor assays; protein concentration by fluorescamine assay with bovine serum albumin as a standard, as is well-known in the art; and, protein heterogeneity by polyacrylamide gel electrophoresis with the protein being detected by silver staining, as also described above. From these assays, the IL-2 receptor from the HUT-102 cells was found to have a specific activity of approximately 2,000 fm receptor/μg protein. The specific activity from the PHA/PBL cells was somewhat less. 

What is claimed is:
 1. Hybridoma ATCC HB 8555 which produces monoclonal antibodies to the human IL-2 receptor.
 2. 2A3 monoclonal antibody (ATCC HB 8555) which specifically binds to the human IL-2 receptor. 